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dc.contributor.authorDomingo de la Rubia, Estela de 
dc.contributor.authorFolcia, César L.
dc.contributor.authorOrtega, Josu
dc.contributor.authorEtxebarria, Jesús
dc.contributor.authorTermine, Roberto
dc.contributor.authorGolemme, Attilio
dc.contributor.authorCoco Cea, Silverio 
dc.contributor.authorEspinet Rubio, Pablo 
dc.date.accessioned2020-09-29T10:28:29Z
dc.date.available2020-09-29T10:28:29Z
dc.date.issued2020
dc.identifier.citationInorganic Chemistry, 2020, 59, 15, 10482–10491es
dc.identifier.issn0020-1669es
dc.identifier.urihttp://uvadoc.uva.es/handle/10324/42651
dc.descriptionProducción Científicaes
dc.description.abstractThis paper reports the synthesis, liquid-crystal behavior, and charge-transport properties in the mesophase of triphenylene Schiff bases and their copper(II), nickel(II), and oxovanadium(IV) complexes. The thermal and electronic properties of the Schiff bases are modulated by coordination to the corresponding metal moieties, which have the ability to self-assemble into linear structures and help the alignment of the triphenylene columns. This produces two kinds of electronically nonconnected columnar regions, one purely organic and one more inorganic. The most remarkable effect is a striking charge mobility enhancement in the metal-containing mesophases, due to the contribution of the more inorganic columns: in comparison to values of hole mobility along the columnar stacking for the purely organic columnar mesophases, on the order of 10–7 cm2 V–1 s–1, these values jump to 1–10 cm2 V–1 s–1 in these hybrid inorganic/organic columnar materials.es
dc.format.mimetypeapplication/pdfes
dc.language.isoenges
dc.publisherAmerican Chemical Societyes
dc.rights.accessRightsinfo:eu-repo/semantics/openAccesses
dc.rights.urihttp://creativecommons.org/licenses/by-nc-nd/4.0/*
dc.subject.classificationMolecular interactionses
dc.titleStriking Increase in Hole Mobility upon Metal Coordination to Triphenylene Schiff Base Semiconducting Multicolumnar Mesophaseses
dc.typeinfo:eu-repo/semantics/articlees
dc.rights.holder© 2019 American Chemical Societyes
dc.identifier.doi10.1021/acs.inorgchem.0c00794es
dc.relation.publisherversionhttps://pubs.acs.org/doi/10.1021/acs.inorgchem.0c00794es
dc.identifier.publicationfirstpage10482es
dc.identifier.publicationissue15es
dc.identifier.publicationlastpage10491es
dc.identifier.publicationtitleInorganic Chemistryes
dc.identifier.publicationvolume59es
dc.peerreviewedSIes
dc.description.projectMinisterio de Ciencia, Innovación y Universidades (Project CTQ2017-89217-P)es
dc.description.projectJunta de Castilla y León (Project VA038G18)es
dc.description.projectUniversidad del País Vasco / EHU (ProjectGIU18/146)es
dc.identifier.essn1520-510Xes
dc.rightsAttribution-NonCommercial-NoDerivatives 4.0 Internacional*
dc.type.hasVersioninfo:eu-repo/semantics/acceptedVersiones


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